Variant #0000037990 (NC_000012.11:g.13768142C>T, NM_000834.3:c.1560G>A (GRIN2B))
| Chromosome |
12 |
| Allele |
Maternal (confirmed) |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.13768142C>T |
| DNA change (hg38) |
g.13615208C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
GRIN2B_000010 |
| Variant remarks |
- |
| Reference |
PubMed: Endele 2010 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
no |
| Frequency |
1/630 cases |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
4.0E-5 View details |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2014-07-01 22:48:45 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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